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Cyclosporin treatment with conversion after three months versus conventional immunosuppression in renal allograft recipients.
- Source :
-
Lancet (London, England) [Lancet] 1987 Mar 14; Vol. 1 (8533), pp. 584-6. - Publication Year :
- 1987
-
Abstract
- In a prospective randomised trial, 72 recipients of cadaver renal allografts received cyclosporin for 3 months followed by azathioprine and prednisone (cyclosporin group), and 71 received azathioprine and prednisone from the day of transplantation (conventional group). Graft survival was better in the cyclosporin group at 3 months and 1 year (93% and 80%) than in the conventional group (83% and 70%). This was not a significant difference. The incidence of acute rejection episodes in the first 3 months was significantly lower in the cyclosporin group (35% versus 77%, p less than 0.00001), as was the number of grafts lost because of immunological failure (1 versus 10, p less than 0.02). After conversion, renal function improved. Only 5 patients had acute rejection after conversion. These episodes were easily reversible in all cases and did not lead to graft loss. The numbers of grafts lost after conversion were similar in the two groups. Conversion of cyclosporin to azathioprine 3 months after renal transplantation is a safe procedure that obviates the long-term toxic effects of cyclosporin.
- Subjects :
- Acute Disease
Adult
Antilymphocyte Serum therapeutic use
Azathioprine administration & dosage
Clinical Trials as Topic
Drug Evaluation
Drug Therapy, Combination
Female
Follow-Up Studies
Graft Survival drug effects
Humans
Infusions, Intravenous
Male
Prednisone administration & dosage
Prospective Studies
Random Allocation
Cyclosporins administration & dosage
Immunosuppressive Agents administration & dosage
Kidney Transplantation
Subjects
Details
- Language :
- English
- ISSN :
- 0140-6736
- Volume :
- 1
- Issue :
- 8533
- Database :
- MEDLINE
- Journal :
- Lancet (London, England)
- Publication Type :
- Academic Journal
- Accession number :
- 2881130
- Full Text :
- https://doi.org/10.1016/s0140-6736(87)90232-7